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FDA 510(k)

SIGNAL PROCESSOR/AVERAGER MODEL 7S11

K-Number: K770878 · 1977-06-01

Decision Date1977-06-01
Product CodeGWJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SIGNAL PROCESSOR/AVERAGER MODEL 7S11 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Systems Corp.. It received FDA 510(k) clearance on 1977-06-01 under 510(k) number K770878. The device is classified under product code GWJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIGNAL PROCESSOR/AVERAGER MODEL 7S11?

SIGNAL PROCESSOR/AVERAGER MODEL 7S11 is a medical device that received FDA 510(k) clearance on 1977-06-01. The listed applicant is Medical Systems Corp.. The 510(k) number is K770878.

When did SIGNAL PROCESSOR/AVERAGER MODEL 7S11 receive FDA 510(k) clearance?

SIGNAL PROCESSOR/AVERAGER MODEL 7S11 received FDA 510(k) clearance on 1977-06-01, under 510(k) number K770878.

Who is the listed applicant for SIGNAL PROCESSOR/AVERAGER MODEL 7S11?

The FDA 510(k) record lists Medical Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIGNAL PROCESSOR/AVERAGER MODEL 7S11?

The FDA product code for SIGNAL PROCESSOR/AVERAGER MODEL 7S11 is GWJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Medical Systems Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 8 devices →

Related Devices (Code: GWJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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